DODGE ( 09V434000 )
November 19, 2009
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TOYOTA ( 09V434000 )
November 19, 2009
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CHEVROLET ( 09V434000 )
November 19, 2009
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INTERNATIONAL ( 09V434000 )
November 19, 2009
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FORD ( 09V434000 )
November 19, 2009
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ENG ( 09V434000 )
November 19, 2009
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ENG Mobile System Recalls
November 19, 2009
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Cardiovascular Systems Recalls ViperSheath Sheath Introducer
November 18, 2009
Cardiovascular Systems, Inc. has announced a voluntary recall of all lots of the ViperSheathTMSheath Introducer on behalf of Thomas Medical due to reports about stretching or fracture of the sheath during use. CSI initiated the nationwide recall on November 2, 2009.
RockHard Laboratories Recalls Specific Lots of RockHard Weekend marketed as Dietary Supplement
November 18, 2009
RockHard Laboratories announced today that it is conducting a voluntary nationwide recall of the company’s dietary supplement sold under the name RockHard Weekend (RHW) specific to the following Lot Numbers:
Blister Pack: T12 705 08 (exp: 10/11) / T12 705 09 (exp: 3/12, 8/12)
3ct Bottle: R417 0509 (exp: 09/12)
8ct Bottle: T237-0509 (exp: 06/12)
SNACKS ON RACKS Issues Nationwide Allergy Alert because of Undeclared Allergens in Their Gourmet Snacks Pack Product Line
November 18, 2009
RECALLS, MARKET WITHDRAWALS, & SAFETY ALERTS ARCHIVE FOR RECALLS, MARKET WITHDRAWALS & SAFETY ALERTS ENFORCEMENT REPORTS INDUSTRY GUIDANCE MAJOR PRODUCT RECALLS – RECALL — FIRM PRESS RELEASE
FDA POSTS PRESS RELEASES AND OTHER NOTICES OF RECALLS AND MARKET WITHDRAWALS FROM THE FIRMS INVOLVED AS A SERVICE TO CONSUMERS, THE MEDIA, AND OTHER INTERESTED PARTIES. FDA DOES NOT ENDORSE EITHER THE PRODUCT OR THE COMPANY.
“Town Hall on Toy Safety”: CPSC Talks to Parents About New Rules Aimed at Making Toys Safer
November 18, 2009
NEW YORK, N.Y. – AT A TOWN HALL MEETING HELD IN NEW YORK CITY, CPSC CHAIRMAN INEZ TENENBAUM WAS JOINED BY PARENTS AND CONSUMERS TO TALK TOY SAFETY. THE DISCUSSION CENTERED AROUND NEW FEDERAL SAFETY RULES THAT ARE IN PLACE FOR TOYS THAT WILL GIVE AMERICAN CONSUMERS GREATER CONFIDENCE WHEN THEY GO SHOPPING THIS HOLIDAY SEASON. CHAIRMAN TENENBAUM INFORMED THE AUDIENCE THAT STARTING THIS YEAR:
Thrive Foods Recalls Assorted Meat And Poultry Products Produced Without Inspection
November 18, 2009
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Nebraska Firm Recalls Fresh Ground Beef Products Due To Possible Ecoli Contamination
November 18, 2009
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Cardiac Science Notifies AED Customers of Nationwide Voluntary Medical Device Correction
November 15, 2009
Cardiac Science Corporation is initiating a voluntary field correction after it was determined certain automated external defibrillators (AEDs) may experience a rare product issue in which the AED may not be able to deliver therapy during a resuscitation attempt. Device failure may affect resuscitation of the patient, which could lead to serious adverse events or death. These AEDs have electronic components which may fail and the failure may not be detected by the device’s periodic self-tests. The affected models include the Powerheart 9300A, 9300C, 9300D, 9300E, 9300P, 9390A, 9390E, and CardioVive 92531, 92532, and 92533 devices.
KENWORTH ( 09V415000 )
November 15, 2009
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GMP Herbal Products Recalls Weight Loss Supplement Found to Contain Undeclared Drug Ingredients
November 14, 2009
GMP Herbal Products, Inc. has been informed by the Food and Drug Administration (FDA) that Pai You Guo, a weight loss dietary supplement, sold and marketed by the firm contains undeclared drug ingredients. FDA lab analyses of dietary supplements distributed by the company were found to contain undeclared sibutramine, an FDA-approved drug used as an appetite suppressant for weight loss; and phenolphthalein, a solution used in chemical experiments and a suspected cancer-causing agent that is not approved for marketing in the United States. The FDA has not approved the Pai You Guo products as drug; therefore the safety and effectiveness of this product is unknown. All lots of the following Pai You Guo product are being recalled. The product is sold either in a box of 30 capsules or a bag of 10 g powder.
Conagra Issues Allergy Alert on a Limited Number of 15 oz. Tubs of Blue Bonnet Light Spread
November 14, 2009
ConAgra Foods, in cooperation with the U.S. Food and Drug Administration (FDA) is voluntarily recalling a limited number of 15 oz. tubs of Blue Bonnet Spread that were inadvertently mispackaged—the lid is for regular Blue Bonnet Spread and the tub portion describes the product as Blue Bonnet Light Spread. The product inside of the tub is regular Blue Bonnet Spread. As a result, the product tubs do not declare the allergen whey (milk), as an ingredient.
IDS Sports Conducts a Voluntary Nationwide Recall of Bromodrol, Dual Action Grow Tabs, Grow Tabs, Mass Tabs, and Ripped Tabs TR
November 14, 2009
IDS Sports announced today that it is conducting a voluntary nationwide recall of five of the company’s dietary supplement products sold under the following names: Bromodrol, Dual Action Grow Tabs, Grow Tabs, Mass Tabs, and Ripped Tabs TR.
Dodge Nitro Recalls: Windshield Wiper Failure
November 14, 2009
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FARBER ( 09V440000 )
November 14, 2009
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